Data / Medical devices / Appliance, Fixation, Spinal Intervertebral Body / France

FDA-registered makers of Appliance, Fixation, Spinal Intervertebral Body in France: 20 establishments

Name: FDA-registered makers of Appliance, Fixation, Spinal Intervertebral Body in France
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

20 establishments in France are registered with the FDA to make Appliance, Fixation, Spinal Intervertebral Body (product code KWQ). 5 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.

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Device: Appliance, Fixation, Spinal Intervertebral Body
Product code: KWQ
Country: France

Makers of Appliance, Fixation, Spinal Intervertebral Body in France

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Source
Clariance-Sas	BEAURAINS Hauts-de-France, France	Complaint file establishment, Manufacturer, Specification developer	2	January 14, 2025	1	api.fda.gov
LDR Medical	Sainte-Savine Aube, France	Specification developer	2	September 29, 2010	0	api.fda.gov
Implanet	Martillac Nouvelle-Aquitaine, France	Manufacturer	1	April 6, 2020	0	api.fda.gov
Microtec SAS	Serres Castet Pyrenees-Atlantiques, France	Manufacturer	1	March 20, 2015	0	api.fda.gov
Spinevision SAS	Antony Hauts-de-Seine, France	Complaint file establishment, Manufacturer	1	November 26, 2001	0	api.fda.gov
Alpes CN SAS	Reignier-Esery Haute-Savoie, France	Contract manufacturer	0		0	api.fda.gov
Charles Pery & Cie	SCIONZIER Haute-Savoie, France	Contract manufacturer	0		0	api.fda.gov
Coulot Decolletage	CHATELLERAULT Vienne, France	Contract manufacturer	0		0	api.fda.gov
Decomicro SAS	Naintre Nouvelle-Aquitaine, France	Contract manufacturer	0		0	api.fda.gov
Euclide Care	Aixe Sur Vienne Haute-Vienne, France	Contract manufacturer	0		0	api.fda.gov
Lopitz Manufacturing	Gradignan Nouvelle-Aquitaine, France	Contract manufacturer	0		0	api.fda.gov
Medical Conteneur SAS	SAINT-SOUPPLETS Seine-et-Marne, France	Contract manufacturer	0		0	api.fda.gov
Medicrea International	RILLIEUX-LA-PAPE Auvergne-Rhone-Alpes, France	Manufacturer	0		0	api.fda.gov
Oury-Guye & Fils	NOGENT Haute-Marne, France	Contract manufacturer	0		0	api.fda.gov
Selenium Medical S.A.S.	La Rochelle Charente-Maritime, France	Contract manufacturer	0		0	api.fda.gov
Simagec	ROUSSET CEDEX Bouches-du-Rhone, France	Contract manufacturer	0		0	api.fda.gov
Simon SAS	Bayeux Calvados, France	Contract manufacturer	0		0	api.fda.gov
Stryker Spine	CESTAS Nouvelle-Aquitaine, France	Contract manufacturer	0		0	api.fda.gov
Symmetry Medical Polyvac SAS	WAMBRECHIES Nord, France	Contract manufacturer	0		0	api.fda.gov
Safe Medical	Fleurieux-Sur-L'Arbresle Rhone, France	Contract manufacturer	0		0	api.fda.gov

Updated November 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.